Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
AngioDynamics Port Catheter Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
AFFF Lawsuit Exposure to firefighting foam chemicals may result in an increased risk of cancer for firefighters, military and airport personnel.
Philips BiPAP Recall Issued Over Risk Plastic in Motor May Release Toxic Chemicals Another Philips BiPAP machine recall has been announced over toxic plastic materials that may release cancer-causing volatile organic compounds (VOC) into user’s airways. August 30, 2022 Russell Maas Add Your Comments Just one year after issuing a massive CPAP/BiPAP recall that impacted millions of sleep apnea machines distributed with a toxic sound abatement foam, which has been linked to thousands of reported injuries among users, Philips has announced yet another BiPAP machine recall, this time involving problems with a plastic component in the motor that can release carcinogenic chemicals into the user’s airway. The Philips BiPAP recall was announced by the U.S. Food and Drug Administration (FDA) on August 29, impacting several models of ventilators that are equipped with a non-compatible material, which may release volatile organic compounds (VOCs) directly into the machine’s air pathways. Officials warn the devices may suddenly shut down without warning if the toxic plastic material enters the motor. In this event, users may not receive sufficient oxygen pressure, which can increase the risk of respiratory injuries. The announcement warns the toxic VOC’s released by the BiPAP machine plastic could cause headache, dizziness, irritation in the eyes, nose, respiratory tract (airway), and skin, hypersensitivity reaction, such as an allergic reaction or another immune system reaction, nausea or vomiting, and toxic cancer-causing effects. However, there are also concerns that chemicals released by the Philips BiPAP may cause cancer and other long-lasting side effects. Problems with Philips CPAP/BiPAP Machines The new recall comes as the manufacturer is still reeling from problems with several million Philips CPAP, BiPAP and ventilator machines distributed between 2009 and April 2021, which were included in a separate recall issued last year. Those machines all included a defective sound abatement foam material, which has been found to degrade and release cancer-causing chemicals and gasses directly into the sleep apnea machine’s tubing, face mask and the lungs of users. Since that recall, thousands of former users have are now pursuing potential Philips CPAP lawsuits, indicating that they have been left with various types of cancer, lung damage and severe respiratory problems following use of the machines to treat sleep apnea. Stay Up-to-Date About Philips CPAP Recall Lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new Philips CPAP recall lawsuit updates or developments. "*" indicates required fields Email* Δ Learn More Stay Up-to-Date About Philips CPAP Recall Lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new Philips CPAP recall lawsuit updates or developments. "*" indicates required fields Email* Δ Learn More This latest Philips recall includes A-Series BiPAP A30 (Ventilator), A-Series BiPAP A40 (Ventilator), A-Series BiPAP V30 (Auto Ventilator) and OmniLab Advanced+ models, which are used in both at-home and clinical environments, such as hospitals and sleep laboratories. The BiPAP machines are designed to pumps air under varying pressure into the airway of the lungs for people with obstructive sleep apnea syndrome to keep their airways open during sleep, and for those who have respiratory insufficiency or respiratory failure. These recalled Philips BiPAP machines were manufactured and distributed for sale throughout the U.S. between August 6, 2020, and September 1, 2021. For now, Philips is recommending users to consult with their healthcare providers to determine whether their plan for care and treatment should change as a result of this recall. While only 386 units are impacted by the recall, officials are warning the A-Series BiPAP A30 (Ventilator) and A-Series BiPAP A40 (Ventilator) machines were also included in the Class I recall of millions of Philips CPAP machines containing toxic PE-PUR sound abatement foam, which have been linked to thousands of adverse events. These models and more than dozen others that contained the PE-PUR foam have already been linked to more than 69,000 reports involving problems among users, including 168 deaths that may be related to breathing particles and gasses released into the machine’s air pathways. Tags: BiPAP, BiPAP Recall, CPAP, CPAP Recall, Philips, Sleep Apnea More Philips CPAP Recall Lawsuit Stories Lawsuits Between Philips and SoClean Over CPAP Machine Problems To Be Trial Ready by July 2025 September 3, 2024 Fairness Hearing For Philips CPAP Recall Medical Monitoring Settlement Set for October July 11, 2024 Philips OmniLab Advanced+ Ventilator Recall Issued Over Loss of Therapy Risks July 1, 2024 2 Comments Allan October 21, 2022 I have sleep apnea and without CPAP my oxygen drops into the 70s and it hurts. First I noticed i kept taking my cpap off during sleep. Later I observed raspy voice, sinus swelling and swelling around eyes. I have been wanting for a replacement to the Philips respironic dream machine CPAP machine about a year. I have been told I am a priority. I assume because I have heart arrhythmias and heart failure with ICD and Polycythemia Vera a bone marrow cancer and diabetic. All 3 conditions are made worse by not using CPAP or inflammation. Also have memory loss from low oxygen from the heart failure and could not pump enough blood to my brain and later a large clot system reducing blood flow from my brain. Which restricted it flowing to my brain. Honestly I can’t afford another event. The type of cancer I have usually kills by clots if you survive that. Other ways. Decreased oxygen accelerates it and no doubt this has shortened my lifespan. Not to mention the worry. I have headaches and raspy voice after use of the machine. Also from sleep Apnea without. Have also developed swelling around eyes. New and concerning problems. Have to take meds to stop fluid build up around my heart. Have had high fevers and coughing up white foam. Taking medical cannabis for pain now. Diabetes is not well controlled which I know untreated sleep apnea makes it worse so does stress and pain. I accidentally fell asleep last night using the machine and used it too long. I feel awful. I wonder. Has this product ruined my best years I have left. What’s worse. Has it taken my last year. Waiting a year just shows the careless attitude Philips respironics has for the safety and wellbeing of its users. Especially those who are seriously ill. Also once I got the machine. It just feels cheaply made. To anyone reading this. Please be vigilant and have any symptoms that could be cancer quickly checked. Cancer is brutally unfair and the pain can be so harsh that you just think you can imagine how bad it can get. It’s much worse. Phillip November 5, 2022 I have a ResMed Air Sense 10. Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes No Post Comment I authorize the above comments be posted on this page Weekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings. Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermPhoneThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Depo-Provera Lawsuit Case Management Conferences Scheduled Throughout 2025 (Posted: today) A federal judge has scheduled regular status conferences for Depo-Provera lawsuits throughout 2025 as part of a strategy to quickly resolve the litigation. 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